Variant report

Variant	nsv1021533
Chromosome Location	chr7:110838612-111201524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2993)
CpG islands
(count:427)
Chromatin interactive
region (count:312)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2993 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
2	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
3	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
4	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
5	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
6	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
7	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
8	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
10	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
11	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
13	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
15	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
16	ARID3A	chr7:110869353-110869485	K562	blood:	n/a	n/a
17	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
18	ARID3A	chr7:110863537-110864343	K562	blood:	n/a	chr7:110863547-110863563 chr7:110863548-110863564
19	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
20	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
21	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
22	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
23	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
24	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
25	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
26	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
27	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
28	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
29	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
30	ATF1	chr7:110889894-110890092	K562	blood:	n/a	n/a
31	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
32	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
33	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
34	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
35	ATF1	chr7:110863987-110864363	K562	blood:	n/a	n/a
36	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
37	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
38	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
39	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
40	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
41	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
42	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
43	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
44	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
46	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
47	ATF3	chr7:111156586-111157138	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
48	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
49	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
50	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111200944-111200994	NB4	blood:	n/a
2	chr7:110879415-110879465	SK-N-MC	brain:	n/a
3	chr7:111200944-111200994	GM19239	blood:	n/a
4	chr7:111198163-111198213	HUVEC	blood vessel:	n/a
5	chr7:111198163-111198213	AG09309	skin:	n/a
6	chr7:111198163-111198213	IMR90	lung:	fetal
7	chr7:111079100-111079150	ECC-1	luminal epithelium:	n/a
8	chr7:110879415-110879465	U87	brain:	n/a
9	chr7:110906785-110906835	SAEC	small airway:	n/a
10	chr7:111033064-111033114	MCF-7	breast:	n/a
11	chr7:111200944-111200994	HRE	kidney:	n/a
12	chr7:111033064-111033114	ovcar-3	ovarian:	n/a
13	chr7:111200944-111200994	RPTEC	kidney:	n/a
14	chr7:111079100-111079150	Hepatocyte	liver:	n/a
15	chr7:111033064-111033114	NHBE	bronchial:	n/a
16	chr7:111033064-111033114	PFSK-1	brain:	n/a
17	chr7:110906785-110906835	NH-A	brain:	n/a
18	chr7:111198163-111198213	HRPEpiC	eye:	n/a
19	chr7:110906785-110906835	HCT-116	colon:	n/a
20	chr7:111079100-111079150	CMK	blood:	n/a
21	chr7:111033064-111033114	PrEC	prostate:	n/a
22	chr7:111086055-111086105	NB4	blood:	n/a
23	chr7:111200944-111200994	HMEC	breast:	n/a
24	chr7:111198163-111198213	SKMC	muscle:	n/a
25	chr7:110906785-110906835	NHDF-neo	bronchial:	n/a
26	chr7:111033064-111033114	GM12878	blood:	n/a
27	chr7:111079100-111079150	T-47D	breast:	n/a
28	chr7:110906785-110906835	ProgFib	skin:	n/a
29	chr7:111086055-111086105	ProgFib	skin:	n/a
30	chr7:111079100-111079150	Jurkat	blood:	n/a
31	chr7:110879415-110879465	GM12892	blood:	n/a
32	chr7:110879415-110879465	IMR90	lung:	fetal
33	chr7:111079100-111079150	SK-N-SH	brain:	n/a
34	chr7:111198163-111198213	NB4	blood:	n/a
35	chr7:111079100-111079150	ovcar-3	ovarian:	n/a
36	chr7:111198163-111198213	HNPCEpiC	eye:	n/a
37	chr7:111198163-111198213	PrEC	prostate:	n/a
38	chr7:111200944-111200994	PFSK-1	brain:	n/a
39	chr7:111033064-111033114	HEK293	kidney:	embryo
40	chr7:110879415-110879465	NH-A	brain:	n/a
41	chr7:111079100-111079150	AG04449	skin:	fetal
42	chr7:111079100-111079150	K562	blood:	n/a
43	chr7:111079100-111079150	HRPEpiC	eye:	n/a
44	chr7:111033064-111033114	GM12891	blood:	n/a
45	chr7:111198163-111198213	HCPEpiC	choroid plexus:	n/a
46	chr7:111079100-111079150	MCF10A-Er-Src	breast:	n/a
47	chr7:111033064-111033114	SK-N-MC	brain:	n/a
48	chr7:111200944-111200994	AoSMC	blood vessel:	n/a
49	chr7:111200944-111200994	HRPEpiC	eye:	n/a
50	chr7:111200944-111200994	ECC-1	luminal epithelium:	n/a

(count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr7:111150255..111152424-chr7:111159146..111160781,2	K562	blood:
2	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
3	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
4	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
5	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
6	chr7:111138086..111139591-chr7:111219192..111221961,2	MCF-7	breast:
7	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
8	chr7:110867615..110870539-chr7:110870998..110875749,6	K562	blood:
9	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
10	chr7:110846499..110848352-chr7:110867218..110869031,2	MCF-7	breast:
11	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
12	chr7:110843078..110844596-chr7:110851457..110854141,2	K562	blood:
13	chr7:110843078..110846205-chr7:110849161..110854141,4	K562	blood:
14	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
15	chr7:111173111..111178494-chr7:111200645..111202653,4	MCF-7	breast:
16	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
17	chr7:111178493..111181177-chr7:111184776..111187564,2	K562	blood:
18	chr7:111050830..111052648-chr7:111066245..111068187,2	K562	blood:
19	chr7:111174213..111177437-chr7:111200487..111202315,3	K562	blood:
20	chr7:111149350..111150943-chr7:111156315..111157965,2	K562	blood:
21	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
22	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
23	chr1:231114585..231115155-chr7:111179137..111179637,2	NB4	blood:
24	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
25	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
26	chr7:110843665..110845702-chr7:110845783..110848771,2	K562	blood:
27	chr7:111168569..111170226-chr7:111188051..111190882,2	K562	blood:
28	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
29	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
30	chr7:110845330..110847607-chr7:110862386..110864699,2	K562	blood:
31	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
32	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
33	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
34	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
35	chr7:110919285..110921892-chr7:110924129..110926222,2	K562	blood:
36	chr7:111115638..111117204-chr7:111120968..111123964,2	K562	blood:
37	chr7:110924432..110926999-chr7:110933691..110937635,4	K562	blood:
38	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
39	chr7:111031028..111033164-chr7:111033658..111035591,2	K562	blood:
40	chr7:110946188..110948736-chr7:111369766..111372546,2	K562	blood:
41	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
42	chr7:110919663..110921773-chr7:111080756..111083394,2	K562	blood:
43	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
44	chr7:111164149..111166792-chr7:111174165..111176807,3	K562	blood:
45	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
46	chr7:111114124..111115929-chr7:111199099..111201690,2	K562	blood:
47	chr7:110975357..110976070-chr7:111125914..111126817,2	K562	blood:
48	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
49	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
50	chr7:111186407..111189009-chr7:111189104..111191721,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-7	chr7:110902289-110902553	expReg_chr7_8342_-

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
IMMP2L	TF binding region
ENSG00000243621	TF binding region
ENSG00000227948	CpG island
IMMP2L	CpG island
ENSG00000243621	CpG island
ENSG00000214188	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000143643	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000136856	chromatin interactions

Extended variants
information (count: 12678 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:12678 , 50 per page) page: 1 2 3 4 5 6 7 ... 254

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148111599	chr7:110838635-110838636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541623251	chr7:110838652-110838653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531040396	chr7:110838668-110838669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553456220	chr7:110838673-110838674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189852289	chr7:110838689-110838690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572007096	chr7:110838720-110838721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115780710	chr7:110838740-110838741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539803724	chr7:110838742-110838743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141916738	chr7:110838839-110838840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146054058	chr7:110838841-110838842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375736456	chr7:110838859-110838860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535324741	chr7:110838879-110838880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182636611	chr7:110838911-110838912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187563213	chr7:110838952-110838953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564817771	chr7:110838972-110838973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35647068	chr7:110838979-110838980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537578308	chr7:110838997-110838998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143049549	chr7:110839034-110839035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557819562	chr7:110839044-110839045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561786947	chr7:110839050-110839051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563899601	chr7:110839084-110839085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140042176	chr7:110839095-110839096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7804926	chr7:110839107-110839108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142629633	chr7:110839164-110839165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370861773	chr7:110839165-110839166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531315212	chr7:110839172-110839173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559850511	chr7:110839173-110839174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573584963	chr7:110839221-110839222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112188375	chr7:110839324-110839325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7808813	chr7:110839344-110839345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375691906	chr7:110839361-110839362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146036724	chr7:110839412-110839413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367907997	chr7:110839413-110839414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544955824	chr7:110839456-110839457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193002678	chr7:110839460-110839461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77798661	chr7:110839491-110839492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570391169	chr7:110839555-110839556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564594984	chr7:110839560-110839561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184656788	chr7:110839574-110839575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546975559	chr7:110839576-110839577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566718539	chr7:110839585-110839586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111701613	chr7:110839592-110839593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7792514	chr7:110839620-110839621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187488112	chr7:110839628-110839629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7809537	chr7:110839641-110839642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568747626	chr7:110839656-110839657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537642214	chr7:110839681-110839682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557617059	chr7:110839757-110839758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577674125	chr7:110839773-110839774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533609064	chr7:110839799-110839800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:2268 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110837400-110840000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:110837600-110839200	Enhancers	HMEC	breast
3	chr7:110837600-110839200	Enhancers	NH-A	brain
4	chr7:110837600-110839200	Enhancers	NHEK	skin
5	chr7:110837600-110839200	Enhancers	NHLF	lung
6	chr7:110837600-110839400	Enhancers	HSMM	muscle
7	chr7:110837600-110839800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:110837600-110840000	Enhancers	Osteobl	bone
9	chr7:110837800-110839000	Enhancers	Hela-S3	cervix
10	chr7:110838000-110838800	Enhancers	HSMMtube	muscle
11	chr7:110838200-110839000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:110838200-110846600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:110838400-110838800	Enhancers	A549	lung
14	chr7:110838400-110839000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:110838400-110839200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:110838400-110839200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:110838400-110839600	Enhancers	NHDF-Ad	bronchial
18	chr7:110838400-110840200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:110838600-110838800	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr7:110838800-110864000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr7:110839000-110839200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:110839200-110839600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:110839600-110840000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:110842400-110842600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
25	chr7:110842600-110852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:110844400-110853000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:110845800-110846000	Enhancers	Left Ventricle	heart
28	chr7:110846000-110864000	Weak transcription	Left Ventricle	heart
29	chr7:110848400-110853000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr7:110850000-110851800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr7:110850400-110851800	Enhancers	Osteobl	bone
32	chr7:110850800-110851400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr7:110850800-110851600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:110850800-110851600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:110851000-110851800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:110851000-110851800	Enhancers	HUVEC	blood vessel
37	chr7:110851200-110851600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr7:110851200-110851600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr7:110851200-110851600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr7:110851200-110851600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:110851200-110851600	Enhancers	NH-A	brain
42	chr7:110851600-110854800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:110852000-110852400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
44	chr7:110852000-110853000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:110852000-110853400	Weak transcription	Pancreas	Pancrea
46	chr7:110852400-110853000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:110852400-110853200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr7:110852400-110853400	Weak transcription	Fetal Intestine Small	intestine
49	chr7:110852800-110853800	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr7:110853000-110853200	Enhancers	Spleen	Spleen

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